User profiles for "author:Bruce H Cohen"

Bruce H. Cohen

Akron Children's Hospital, Professor of Pediatrics, Northeast Ohio Medical University
Verified email at akronchildrens.org
Cited by 11128

[HTML][HTML] Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

S Parikh, A Goldstein, MK Koenig, F Scaglia… - Genetics in …, 2015 - nature.com
Purpose: The purpose of this statement is to review the literature regarding mitochondrial
disease and to provide recommendations for optimal diagnosis and treatment. This …

The in-depth evaluation of suspected mitochondrial disease

TMMS Committee, RH Haas, S Parikh, MJ Falk… - Molecular genetics and …, 2008 - Elsevier
Mitochondrial disease confirmation and establishment of a specific molecular diagnosis
requires extensive clinical and laboratory evaluation. Dual genome origins of mitochondrial …

A modern approach to the treatment of mitochondrial disease

S Parikh, R Saneto, MJ Falk, I Anselm… - … treatment options in …, 2009 - Springer
Opinion statement The treatment of mitochondrial disease varies considerably. Most experts
use a combination of vitamins, optimize patients' nutrition and general health, and prevent …

[PDF][PDF] Treatment of children with medulloblastomas with reduced-dose craniospinal radiation therapy and adjuvant chemotherapy: A Children's Cancer Group Study

RJ Packer, J Goldwein, HS Nicholson… - Journal of clinical …, 1999 - researchgate.net
Purpose: Medulloblastoma is the most common malignant brain tumor of childhood. After
treatment with surgery and radiation therapy, approximately 60% of children with …

Outcome for children with medulloblastoma treated with radiation and cisplatin, CCNU, and vincristine chemotherapy

RJ Packer, LN Sutton, R Elterman, B Lange… - Journal of …, 1994 - thejns.org
✓ It has previously been reported in a single-institution trial that progression-free survival of
children with medulloblastoma treated with radiotherapy and 1-(2-chloroethyl)-3-cyclohexyl …

Mitochondrial disease: a practical approach for primary care physicians

RH Haas, S Parikh, MJ Falk, RP Saneto, NI Wolf… - …, 2007 - publications.aap.org
Notorious variability in the presentation of mitochondrial disease in the infant and young
child complicates its clinical diagnosis. Mitochondrial disease is not a single entity but …

Intracranial germ cell tumors

RJ Packer, BH Cohen, K Cooney - The oncologist, 2000 - academic.oup.com
Intracranial germ cell tumors are a heterogeneous group of lesions which occur in children
and adults. Within the classification of intracranial germ cell tumors, there are a variety of …

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

LJC Wong, RK Naviaux, N Brunetti‐Pierri… - Human …, 2008 - Wiley Online Library
Mutations in the POLG gene have emerged as one of the most common causes of inherited
mitochondrial disease in children and adults. They are responsible for a heterogeneous …

[HTML][HTML] Mitochondrial disease in autism spectrum disorder patients: a cohort analysis

JR Weissman, RI Kelley, ML Bauman, BH Cohen… - PloS one, 2008 - journals.plos.org
Background Previous reports indicate an association between autism spectrum disorders
(ASD) and disorders of mitochondrial oxidative phosphorylation. One study suggested that …

[HTML][HTML] Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

S Parikh, A Goldstein, A Karaa, MK Koenig, I Anselm… - Genetics in …, 2017 - Elsevier
The purpose of this statement is to provide consensus-based recommendations for optimal
management and care for patients with primary mitochondrial disease. This statement is …